β-Pyridylenolate zinc catalysts for the ring-opening homo- and copolymerization of ε-caprolactone and lactides

A family of zinc beta-pyridylenolates with varying alpha, beta-substituents has been synthesized. A direct reaction of beta-pyridyl ketone ligands with ZnEt2 in toluene afforded dimeric [LZnEt](2) (L = (2-C5H4N)-C(R-1)= C(R-2)-O-). X-ray structural data revealed that all the [LZnEt](2) complexes exist as mu-O-bridged dimers in the solid state, although they adopt a different geometry. Each of the [LZnEt](2) complexes is a highly active catalyst for the ring-opening polymerization (ROP) of e-caprolactone (epsilon-CL) and racemic lactide (rac-LA), respectively. The donating group on the enolate ligand can accelerate the ROP reaction and control the polymerization process well. All complexes also showed different abilities in the block and random copolymerization of e epsilon-CL and L-LA. Diblock PCL-b-PLLA and PLLA-b-PCL copolymers were easily prepared via sequential addition of epsilon-CL and L-LA by using complex 10, respectively. Random copolymers of PCL-ranPLLA were also synthesized from complex 10. The copolymers of PCL-ran-PLLA were shown to possess monomer contents which matched well with their composition in the monomer feed. NMR and DSC characterization confirmed a highly random structure of these copolymers, resulting in closely average lengths of the caproyl and lactidyl sequences (L-CL = 2.1; L-LA = 1.9). All zinc complexes as efficient singlecomponent initiators in both homo-and copolymerizations showed that polymers were probably susceptible to chain transfer and transesterification due to the close Zn...Zn proximity in the dimer. The polymers initiated by [LZnEt](2) in the absence of BnOH showed high molecular weight and narrow molecular weight distributions.